Literature DB >> 14647956

Alcohol intoxication increases allopregnanolone levels in male adolescent humans.

J M Torres1, E Ortega.   

Abstract

RATIONALE: Teenage drinking is a cause of growing concern in industrialized countries, where almost 35% of alcohol drinkers are under 16 years old. Increased anxiety, irritability and depression among adolescents may induce them to seek the anxiolytic and rewarding properties of alcohol. Allopregnanolone is rewarding in rodents, and therefore may contribute to the effects of alcohol.
OBJECTIVE: In this paper, we studied the effects of acute alcohol intoxication on the plasma levels of allopregnanolone in male adolescents.
METHODS: Blood samples were drawn from male adolescents who arrived at the Emergency Department of the Hospital. Two groups were studied: one study group was formed by adolescents who arrived with evident behavioral symptoms of acute alcohol intoxication (AAI) and the other by those arriving for mild trauma (contusions, sprains) after no consumption of alcohol (Controls).
RESULTS: Our results demonstrate that AAI significantly increases serum allopregnanolone levels in male adolescents.
CONCLUSIONS: Because alcohol and allopregnanolone positively modulate gamma-aminobutyric acid type A (GABAA) receptors, allopregnanolone may play a major role in the anxiolytic and rewarding effects of alcohol, either directly or by influencing the sensitivity of GABAA receptors to alcohol.

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Year:  2003        PMID: 14647956     DOI: 10.1007/s00213-003-1662-0

Source DB:  PubMed          Journal:  Psychopharmacology (Berl)        ISSN: 0033-3158            Impact factor:   4.530


  21 in total

Review 1.  Ethanol and neurosteroid interactions in the brain.

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6.  Dimensions of adolescent problem drinking.

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7.  Effects of acute alcohol intoxication on pituitary-gonadal axis hormones, pituitary-adrenal axis hormones, beta-endorphin and prolactin in human adolescents of both sexes.

Authors:  J Frias; R Rodriguez; J M Torres; E Ruiz; E Ortega
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  36 in total

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Review 4.  GABAergic contributions to alcohol responsivity during adolescence: insights from preclinical and clinical studies.

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5.  Cellular GABAergic Neuroactive Steroid (3α,5α)-3-Hydroxy-Pregnan-20-One (3α,5α-THP) Immunostaining Levels Are Increased in the Ventral Tegmental Area of Human Alcohol Use Disorder Patients: A Postmortem Study.

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Review 6.  Divergent neuroactive steroid responses to stress and ethanol in rat and mouse strains: relevance for human studies.

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Review 7.  GABAA receptor polymorphisms in alcohol use disorder in the GWAS era.

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9.  Inhibition of 5alpha-reduced steroid biosynthesis impedes acquisition of ethanol drinking in male C57BL/6J mice.

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Review 10.  Manipulation of GABAergic steroids: Sex differences in the effects on alcohol drinking- and withdrawal-related behaviors.

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